Regulatory Affairs is a critical field that ensures companies comply with the laws and regulations governing the development and marketing of products, particularly in the pharmaceutical and medical device industries. Professionals in this area work closely with government agencies like the FDA to facilitate the approval process for new products, ensuring they meet safety and efficacy standards. The role of Regulatory Affairs extends beyond just compliance; it involves strategic planning and communication with various stakeholders. By navigating complex regulatory landscapes, these professionals help bring innovative therapies and technologies to market, ultimately improving patient outcomes and public health.